510(k) Report

510(k) · Cleared

Cleared

Noblus Ultrasound Diagnostic System

K130308510(k) SpecialCleared Apr 5, 201357-day reviewClass II21 CFR 892.1550

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Hitachi Aloka Medical, Ltd. · IYN System, Imaging, Pulsed Doppler, Ultrasonic

Cleared on Apr 5, 2013 as substantially equivalent to K102901 (Hitachi Medical Systems America, Inc., 2010) after a 57-day review. Its family tree reaches back 13 generations to 1995. 59 later devices descend from it.

Decided
Apr 5, 2013
Review
57 days
Class
Class II
Product code
IYN
Recalls
None
Predicates
1

Its longest line of descent runs back 13 generations to K935595 (1995). 68 ancestors in all, the oldest K891689 (1989). 59 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2008: 1 other ancestor2006: 2 other ancestors2007: 1 other ancestor2003: 5 other ancestors2005: 5 other ancestors2004: 9 other ancestors2001: 4 other ancestors2000: 5 other ancestors2002: 4 other ancestors1995: 4 other ancestors1999: 5 other ancestors1998: 1 other ancestor1997: 3 other ancestors1994: 4 other ancestors1992: 1 other ancestor1989: 1 other ancestor2015: 1 descendant cleared2018: 7 descendants cleared2016: 5 descendants cleared2017: 1 descendant cleared2019: 7 descendants cleared2020: 6 descendants cleared2022: 8 descendants cleared2021: 8 descendants cleared2023: 5 descendants cleared2024: 5 descendants cleared2026: 4 descendants cleared2025: 2 descendants clearedK935595 · Acuson Model 3001 · Acuson Corp. · 1995K973767 · Harmonic Imaging with Contrast · Acuson Corp. · 1997K022567 · Sequoia Signature II Diagnostic Ultrasound System · Acuson Corp. · 2002K032114 · Sequoia 8.0 Diagnostic Ultrasound System · Siemens Medical Solutions USA, Inc. · 2003×3: 3 generations cleared close together, K041319 (2004), K042770 (2004), K050240 (2005) K052894 · Sonoline G60 S Ultrasound System · Siemens Medical Solutions USA, Inc. · 2005 · recalled×2: 2 generations cleared close together, K063138 (2006), K063803 (2007) K072786 · Acuson S2000 Ultrasound System · Siemens Medical Solutions USA, Inc. · 2007×2: 2 generations cleared close together, K093466 (2010), K102901 (2010) 1990200020102020
Other ancestors, by generationDescendants, by generation 3 generations back: 2 other ancestors4 generations back: 3 other ancestors5 generations back: 8 other ancestors6 generations back: 6 other ancestors7 generations back: 8 other ancestors8 generations back: 9 other ancestors9 generations back: 9 other ancestors10 generations back: 10 other ancestors 1 generation forward: 1 descendant2 generations forward: 7 descendants3 generations forward: 4 descendants4 generations forward: 8 descendants5 generations forward: 10 descendants6 generations forward: 9 descendants7 generations forward: 7 descendants8 generations forward: 4 descendants9 generations forward: 2 descendants10 generations forward: 4 descendants11 generations forward: 2 descendants12 generations forward: 1 descendant K102901 · HI Vision Avius Diagnostic Ultrasound Scanner · Hitachi Medical Systems America, Inc. · 2010 · recalledK093466 · HI Vision Preirus Doagnostic Ultrasound Scanner Model HI Vision Preirus · Hitachi Medical Systems America, Inc. · 2010 · recalledK072786 · Acuson S2000 Ultrasound System · Siemens Medical Solutions USA, Inc. · 2007K063803 · Acuson Antares Diagnostic Ultrasound System · Siemens Medical Solutions USA, Inc., Ultrasound DI · 2007 · recalledK063138 · Modification to Acuson Antares Ultrasound System · Siemens Medical Solutions USA, Inc. · 2006K052894 · Sonoline G60 S Ultrasound System · Siemens Medical Solutions USA, Inc. · 2005 · recalledK050240 · Modification to Acuson CV70 Cardiovascular System · Siemens Medical Solutions USA, Inc. · 2005 · recalledK042770 · Modification to Acuson CV70 Cardiovascular System · Siemens Medical Solutions USA, Inc. · 2004 · recalledK041319 · Sequoia Diagnostic Ultrasound System · Siemens Medical Solutions USA, Inc. · 2004K032114 · Sequoia 8.0 Diagnostic Ultrasound System · Siemens Medical Solutions USA, Inc. · 2003K022567 · Sequoia Signature II Diagnostic Ultrasound System · Acuson Corp. · 2002K973767 · Harmonic Imaging with Contrast · Acuson Corp. · 1997K935595 · Acuson Model 3001 · Acuson Corp. · 1995−10−50+5+10
  1. Root · 13 generations backK935595 Acuson Model 3001Acuson Corp. · 1995
  2. 9 generations between
  3. 3 generations backK072786 Acuson S2000 Ultrasound SystemSiemens Medical Solutions USA, Inc. · 2007
  4. 2 generations backK093466 HI Vision Preirus Doagnostic Ultrasound Scanner Model HI Vision…Hitachi Medical Systems America, Inc. · 2010 · Recalled
  5. 1 generation backK102901 HI Vision Avius Diagnostic Ultrasound ScannerHitachi Medical Systems America, Inc. · 2010 · Recalled
  6. This deviceK130308 Noblus Ultrasound Diagnostic SystemHitachi Aloka Medical, Ltd. · 2013
  7. Descendant · cites it directly · 58 of its ownK142368 Noblus Diagnostic Ultrasound ScannerHitachi Aloka Medical, Ltd. · 2015 · Recalled
  8. Descendant · 2 generations on · 50 of its ownK171048 RS80A Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2017
  9. Descendant · 3 generations on · 39 of its ownK173204 RS85 Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2018
  10. Descendant · 2 generations on · 32 of its ownK173513 WS80A Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2018 · Recalled
  11. Descendant · 3 generations on · 31 of its ownK181336 HS50 / HS60 Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2018
Show all 13 generations
  1. Root · 13 generations backK935595 Acuson Model 3001Acuson Corp. · 1995
  2. 12 generations backK973767 Harmonic Imaging with ContrastAcuson Corp. · 1997
  3. 11 generations backK022567 Sequoia Signature II Diagnostic Ultrasound SystemAcuson Corp. · 2002
  4. 10 generations backK032114 Sequoia 8.0 Diagnostic Ultrasound SystemSiemens Medical Solutions USA, Inc. · 2003
  5. 9 generations backK041319 Sequoia Diagnostic Ultrasound SystemSiemens Medical Solutions USA, Inc. · 2004
  6. 8 generations backK042770 Modification to Acuson CV70 Cardiovascular SystemSiemens Medical Solutions USA, Inc. · 2004 · Recalled
  7. 7 generations backK050240 Modification to Acuson CV70 Cardiovascular SystemSiemens Medical Solutions USA, Inc. · 2005 · Recalled
  8. 6 generations backK052894 Sonoline G60 S Ultrasound SystemSiemens Medical Solutions USA, Inc. · 2005 · Recalled
  9. 5 generations backK063138 Modification to Acuson Antares Ultrasound SystemSiemens Medical Solutions USA, Inc. · 2006
  10. 4 generations backK063803 Acuson Antares Diagnostic Ultrasound SystemSiemens Medical Solutions USA, Inc., Ultrasound DI · 2007 · Recalled
  11. 3 generations backK072786 Acuson S2000 Ultrasound SystemSiemens Medical Solutions USA, Inc. · 2007
  12. 2 generations backK093466 HI Vision Preirus Doagnostic Ultrasound Scanner Model HI Vision…Hitachi Medical Systems America, Inc. · 2010 · Recalled
  13. 1 generation backK102901 HI Vision Avius Diagnostic Ultrasound ScannerHitachi Medical Systems America, Inc. · 2010 · Recalled
  14. This deviceK130308 Noblus Ultrasound Diagnostic SystemHitachi Aloka Medical, Ltd. · 2013

Showing 5 of 59 descendants. See all descendants

Descendants cleared per year

2015: 12016: 52017: 12018: 72019: 72020: 62021: 82022: 82023: 52024: 52025: 22026: 4
2015high 8 (2021) · low 1 (2015)2026

Most influential descendants

Showing 5 of 59 · See all
  • K142368Noblus Diagnostic Ultrasound ScannerHitachi Aloka Medical, Ltd. · 2015 · cites it directly58descendants
  • K171048RS80A Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2017 · 2 generations on50descendants
  • K173204RS85 Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2018 · 3 generations on39descendants
  • K173513WS80A Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2018 · 2 generations on32descendants
  • K181336HS50 / HS60 Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2018 · 3 generations on31descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−13K935595Acuson Model 3001Acuson Corp.1995—
−12K973767Harmonic Imaging with ContrastAcuson Corp.1997—
−11K022567Sequoia Signature II Diagnostic Ultrasound SystemAcuson Corp.2002—
−10K032114Sequoia 8.0 Diagnostic Ultrasound SystemSiemens Medical Solutions USA, Inc.2003—
−9K041319Sequoia Diagnostic Ultrasound SystemSiemens Medical Solutions USA, Inc.2004—
−8K042770Modification to Acuson CV70 Cardiovascular SystemSiemens Medical Solutions USA, Inc.20041
−7K050240Modification to Acuson CV70 Cardiovascular SystemSiemens Medical Solutions USA, Inc.20051
−6K052894Sonoline G60 S Ultrasound SystemSiemens Medical Solutions USA, Inc.20051
−5K063138Modification to Acuson Antares Ultrasound SystemSiemens Medical Solutions USA, Inc.2006—
−4K063803Acuson Antares Diagnostic Ultrasound SystemSiemens Medical Solutions USA, Inc., Ultrasound DI20079
−3K072786Acuson S2000 Ultrasound SystemSiemens Medical Solutions USA, Inc.2007—
−2K093466HI Vision Preirus Doagnostic Ultrasound Scanner Model HI Vision PreirusHitachi Medical Systems America, Inc.20101
−1K102901HI Vision Avius Diagnostic Ultrasound ScannerHitachi Medical Systems America, Inc.20101
0 (this device)K130308Noblus Ultrasound Diagnostic SystemHitachi Aloka Medical, Ltd.2013—
+1K142368Noblus Diagnostic Ultrasound ScannerHitachi Aloka Medical, Ltd.20151
+2K171048RS80A Diagnostic Ultrasound SystemSamsung Medison Co., Ltd.2017—
+3K173204RS85 Diagnostic Ultrasound SystemSamsung Medison Co., Ltd.2018—
+2K173513WS80A Diagnostic Ultrasound SystemSamsung Medison Co., Ltd.20181
+3K181336HS50 / HS60 Diagnostic Ultrasound SystemSamsung Medison Co., Ltd.2018—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198910
199210
199440
199540
199730
199810
199950
200050
200140
200240
200350
200490
200550
200620
200710
200810

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201510
201650
201710
201870
201970
202060
202180
202280
202350
202450
202520
202640
FIG. 1 — Lineage of K130308, 1995–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in IYN? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new IYN device

  1. #1 K240850 EPIQ Series Diagnostic Ultrasound Systems…score 32.1 · 24 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K102901HI Vision Avius Diagnostic Ultrasound Scanner
Summary page 1
…Classification name - System, Imaging, Pulsed Doppler, Ultrasonic 3. Substantially Equivalent Device(s): Hitachi HI VISION Avius Diagnostic Ultrasound Scanner (K102901] 4. Device Description: An ultrasound diagnostic system with the following features: o Ultrasound transducer(…
Hitachi Medical Systems America, Inc.20101

What descends from it? (59)

See all 59

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K142368Noblus Diagnostic Ultrasound ScannerHitachi Aloka Medical, Ltd.201558

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 18 years and passes through 5 companies; a new generation was cleared every 11 months on median.
  • 18 of the 68 ancestors have a recall of any class.
  • Of its descendants, K142368 (Hitachi Aloka Medical, Ltd., 2015) has gone furthest, with 58 descendants of its own.

How does its category compare?

All IYN devices

IYN System, Imaging, Pulsed Doppler, Ultrasonic: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.

FDA decisions per year · IYN

57in 2025

2007: 132008: 252009: 182010: 292011: 392012: 432013: 512014: 562015: 542016: 602017: 642018: 592019: 472020: 572021: 462022: 532023: 442024: 502025: 572026 (partial year): 44
2007high 64 (2017) · low 13 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · IYN

124in 2025

2007: 26 days median2008: 18 days median2009: 29 days median2010: 67 days median2011: 46 days median2012: 37 days median2013: 60 days median2014: 39 days median2015: 55 days median2016: 56 days median2017: 83 days median2018: 85 days median2019: 79 days median2020: 72 days median2021: 105 days median2022: 105 days median2023: 115 days median2024: 119 days median2025: 124 days median2026 (partial year): 107 days median
2007high 124 (2025) · low 18 (2008)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · IYN

10in 2025

2007: 162008: 122009: 82010: 102011: 82012: 32013: 82014: 22015: 32016: 22018: 72020: 42021: 82022: 102023: 42024: 12025: 102026 (partial year): 2, 1 Class I
2007high 16 (2007) · low 0 (2017)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · IYN

610in 2025

2007: 32008: 22009: 92010: 172011: 182012: 202013: 182014: 482015: 1162016: 1452017: 1462018: 852019: 592020: 672021: 2132022: 1862023: 2292024: 2662025: 610
2007high 610 (2025) · low 2 (2008)2025

MAUDE reports naming product code IYN, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20071326163
20082518122
2009182989
201029671017
20113946818
20124337320
20135160818
20145639248
201554553116
201660562145
201764830146
20185985785
20194779059
20205772467
2021461058213
20225310510186
2023441154229
2024501191266
20255712410610
2026441072 (1)—

What is it indicated for?

The Noblusm Ultrasound Diagnostic System is intended for use by trained personnel (doctor, sonographer, etc.) for the diagnostic ultrasound evaluation of Abdominal, Cardiac, Intra-operative, Fetal, Pediatric, Small Organ, Peripheral vessel, Biopsy, Trans-rectal, Trans-vaginal, Musculoskeletal, Neonatal Cephalic. Adult Cephalic, Endloscopy, Intra-luminal, Gynecology, Urology, and Laparoscopic clinical applications. The Modes of Operation of the Noblusm…

Read the full statement (91 words)

The Noblusm Ultrasound Diagnostic System is intended for use by trained personnel (doctor, sonographer, etc.) for the diagnostic ultrasound evaluation of Abdominal, Cardiac, Intra-operative, Fetal, Pediatric, Small Organ, Peripheral vessel, Biopsy, Trans-rectal, Trans-vaginal, Musculoskeletal, Neonatal Cephalic. Adult Cephalic, Endloscopy, Intra-luminal, Gynecology, Urology, and Laparoscopic clinical applications.

The Modes of Operation of the Noblusm Ultrasound Diagnostic System are B mode, M mode, PW mode (Pulse Wave Doppler), CW mode (Continuous Wave Doppler), Color Doppler, Amplitude Doppler (Color Flow Angiography), TDI (Tissue Doppler Imaging), 3D Imaging, 4D Imaging, and Real Time Tissue Elastography.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K130308: Noblus Ultrasound Diagnostic System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K130308

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026